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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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UV Smart D25 — 1 UDI-DI variant, MDR (UV Smart Technologies B.V.)

MD Atlas
UV Smart Technologies B.V.

Data from EUDAMED, last updated May 30, 2026

UV Smart D25

87193266342D253N

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: UV Smart Technologies B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 87193266342D253N
Device name: UV Smart D25
Device model: V2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: UV Smart Technologies B.V.
SRN: NL-MF-000017126
Country: Netherlands
Email: info@uvsmart.nl
Phone: 0850609800

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GVNFJBHHVASKQ15RCYTNK9BQ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

D2508719326634265